Platform evidence & partner programmes Preclinical platform
Platform pipeline

One controllable payload. Multiple partner programmes.

GenLumina is developing a light-activated intracellular payload that can be combined with different antibodies, peptides or ligands. Our internal programmes generate evidence for the platform. Pharmaceutical partners can then evaluate the same payload with targeting biology relevant to their own pipelines.

Dual-control architecture

Selectivity is built in twice.

Molecular targeting Antibody, peptide or ligand
GenLumina payload Proprietary light-activated platform
Spatial activation Light controls where cytotoxic activity is activated
01 · Internal evidence programmes

Starting points that demonstrate platform breadth.

GL-001 and GL-002 are internal evidence programmes used to validate different targeting modalities, tumor settings and development questions. They demonstrate what the platform can do; they do not limit GenLumina to these targets or indications.

This is a platform pipeline—not a closed two-asset drug pipeline.

Internal programmes generate transferable knowledge around conjugation, uptake, intracellular localization, controlled activation, safety and efficacy. New programmes can be created around targeting biology selected by pharmaceutical partners.

Internal evidence → partner-specific programmes
Evidence programme Targeting Discovery Preclinical Clinical Collaboration
GL-002 · Internal evidence

HER2

HER2-expressing solid tumors

Demonstrates antibody-targeted platform application
Antibody-targeted GenLumina platform Anti-HER2 mAb
Discovery Target & construct defined
Preclinical Current evidence focus
Clinical Subject to further validation
Collaboration Open for collaboration
Partner programme template

Your targeting biology can become the next programme.

A pharma or biotech partner does not need to adopt GL-001 or GL-002. It can bring an antibody, peptide or ligand from its own pipeline and evaluate the GenLumina payload in a separately defined proof-of-concept programme.

01 · Partner Antibody, peptide or ligand
02 · GenLumina Conjugation with light-activated payload
03 · PoC Partner-specific validation
04 · Decision Option to license
05 · Programme Indication- and territory-specific licence
02 · Platform logic

A pipeline designed to expand through partners.

Shared core

One controllable payload

The same light-activated intracellular payload can be evaluated across multiple targeting approaches and indications.

Flexible targeting

Partner-owned biology

Antibodies, peptides or ligands can be selected around each partner's existing pipeline, target biology and indication priorities.

Separate programmes

Programme by programme

Each combination can follow its own PoC, decision criteria, financing and indication-specific licensing route.

Platform ownership

GenLumina retains the core

Programme-specific rights can be licensed while GenLumina preserves ownership of the underlying payload platform for additional partners and applications.

03 · What advances a programme

Evidence before expansion.

Internal and partner programmes progress through the same evidence logic. The objective is to answer specific technical and biological questions before larger development commitments or commercial rights are triggered.

Step 1

Conjugation & stability

Confirm construct quality, stability and reproducibility with the selected targeting molecule.

Can we build it reliably?
Step 2

Uptake & localization

Assess binding, internalization and intracellular localization in the relevant tumor model.

Does it reach the intended cells?
Step 3

Activation & selectivity

Measure controlled light activation, tumor-cell killing and selectivity against agreed criteria.

Does spatial activation add value?
Step 4

Advance or stop

Use the combined evidence to determine whether the programme should progress to in-vivo validation and the agreed option-to-license pathway.

Joint programme decision
04 · Add a programme

Bring your targeting biology.

GenLumina can define a focused PoC around an antibody, peptide or ligand relevant to your pipeline. We can agree upfront which scientific criteria should determine whether a successful programme progresses toward an indication- and territory-specific licensing option.

Explore partnering →